Cas 1415212-15-5,7-(2,5-dimethoxybenzylidene)-4-(2,5-dimethoxyphenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-2(5H)-one

1415212-15-5

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Basic information

Product Name: 7-(2,5-dimethoxybenzylidene)-4-(2,5-dimethoxyphenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-2(5H)-one
Synonyms: 7-(2,5-dimethoxybenzylidene)-4-(2,5-dimethoxyphenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-2(5H)-one
CAS NO:1415212-15-5
Molecular Formula:
Molecular Weight: 422.481
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 7-(2,5-dimethoxybenzylidene)-4-(2,5-dimethoxyphenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-2(5H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 7-(2,5-dimethoxybenzylidene)-4-(2,5-dimethoxyphenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-2(5H)-one(1415212-15-5)
EPA Substance Registry System: 7-(2,5-dimethoxybenzylidene)-4-(2,5-dimethoxyphenyl)-3,4,6,7-tetrahydro-1H-cyclopenta[d]pyrimidin-2(5H)-one(1415212-15-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1415212-15-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415212-15-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,2,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1415212-15:
(9*1)+(8*4)+(7*1)+(6*5)+(5*2)+(4*1)+(3*2)+(2*1)+(1*5)=105
105 % 10 = 5
So 1415212-15-5 is a valid CAS Registry Number.

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1415212-15-5Relevant academic research and scientific papers

Synthesis of substituted pyrimidinones catalyzed by boric acid and glycerol in aqueous medium

Mukhopadhyay, Chhanda,Datta, Arup

, p. 438 - 449 (2013)

An expeditious one-pot synthesis of substituted pyrimidinone derivatives with aromatic aldehydes, cyclopentanone, and urea (or thiourea) was developed with boric acid (10mol%) and glycerol (0.1mL) in aqueous medium at 45-50 C. The methodology is simple, h

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